Patent foramen ovale
Symptom Information:
Symptom ID: | HPO:0001655 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of cardiac atrium(HPO:0005120) Atria septal defect(HPO:0001631) Patent foramen ovale(HPO:0001655) Abnormality of the cardiac septa(HPO:0001671) Abnormality of the atrial septum(HPO:0011994) Atria septal defect(HPO:0001631) Patent foramen ovale(HPO:0001655) MedDRA: |
||||
Database Frequency: | 31 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
1p36 deletion syndrome | (Orphanet:1606) |
ATRIAL SEPTAL DEFECT 4 | (OMIM:611363) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Distal monosomy 6p | (Orphanet:96125) |
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 | (OMIM:615539) |
FIBROCHONDROGENESIS 1 | (OMIM:228520) |
Familial long QT syndrome | (Orphanet:768) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Fibrochondrogenesis | (Orphanet:2021) |
HYPERTELORISM AND TETRALOGY OF FALLOT | (OMIM:239711) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypoplastic left heart syndrome 2 | (OMIM:614435) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Neonatal hemochromatosis | (Orphanet:446) |
Nephronophthisis 9 | (OMIM:613824) |
Neu-Laxova syndrome | (Orphanet:2671) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
RIENHOFF SYNDROME | (OMIM:615582) |
RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL | (OMIM:610338) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Timothy syndrome | (Orphanet:65283) |
Transaldolase deficiency | (Orphanet:101028) |
Transketolase deficiency | (ORPHA:488618) |